| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:92134711-92134890 | Common:3; Rare:54 | ||||
| chr7:92245843-92245966 | Rare:34; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92528385-92528813 | Common:3; Rare:134; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92590046-92590123 | Rare:31 | ||||
| chr7:93117929-93118082 | Rare:25 | ||||
| chr7:93232201-93232389 | Common:2; Rare:34 | ||||
| chr7:93890650-93890983 | Common:4; Rare:94 | ||||
| chr7:93921656-93922178 | Common:7; Rare:125 | ||||
| chr7:94004294-94004507 | Rare:59 | ||||
| chr7:94394194-94394360 | Common:1; Rare:34 | ||||
| chr7:94394543-94395096 | Common:1; Rare:103; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:94425766-94426052 | Rare:87; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:94656118-94656424 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:95434893-95435206 | Common:1; Rare:126; Clinvar (benign):1 | ||||
| chr7:95596283-95596337 | Rare:23 |